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Nuvasive, Inc.

United States·US-MF-000007421

Last updated September 17, 2026

Information

Country: United States
Address: 7475, Lusk Blvd, San Diego, United States
Website: https://www.globusmedical.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: +1-858-909-1800
PRRC Contact: Daniel S. Paul
EUDAMED SRN: US-MF-000007421
FDA FEI Number: 3002980729
DUNS Number: 053950783

Catalogue (44291)

Page 28 of 500

Device	Model / Reference	Registries	Class	Status
Xlif	6999138	FDA UDI	Class I	Active
ReLine	11000454	FDA UDI	Class II	Active
ReLine	14581120	FDA UDI	Class II	Active
ReLine	14515530	FDA UDI	Class II	Active
ReLine	16118060	FDA UDI	Class II	Active
CoRoent	5294328	FDA UDI	Class II	Active
Brigade	6968515	FDA UDI	Class II	Active
Modulus	1114308P2	FDA UDI	Class II	Active
ReLine	14584520	FDA UDI	Class II	Active
ReLine	13216580	FDA UDI	Class II	Active
X-Core	7160035P2	FDA UDI	Class II	Active
ReLine	16178575	FDA UDI	Class II	Active
X-Core	6539010	FDA UDI	Class I	Active
ReLine	24014570	FDA UDI	Class II	Active
VuePoint	8976518	FDA UDI	Class II	Active
Cohere	8260845P2	FDA UDI	Class II	Active
ReLine	3776518	FDA UDI	Class II	Active
Brigade	1903302	FDA UDI	Class II	Active
CoRoent	5193285	FDA UDI	Class II	Active
ReLine	13174045	FDA UDI	Class II	Active
CoRoent	5201300	FDA UDI	Class II	Active
ReLine	16082555	FDA UDI	Class II	Active
Precept	8847095	FDA UDI	Class II	Active
ReLine	24012560	FDA UDI	Class II	Active
ReLine	3837034	FDA UDI	Class II	Active
Modulus	1225055P2	FDA UDI	Class II	Active
CoRoent	6421655P2	FDA UDI	Class II	Active
CoRoent	6312250CP2	FDA UDI	Class II	Active
ReLine	12455030	FDA UDI	Class II	Active
CoRoent	5113328	FDA UDI	Class II	Active
ReLine	13066025	FDA UDI	Class II	Active
ReLine	16022570	FDA UDI	Class II	Active
Gradient	7460505	FDA UDI	Class II	Active
Armada	8549510	FDA UDI	Class II	Active
ReLine	14155100	FDA UDI	Class II	Active
ReLine	10000889	FDA UDI	Class I	Active
CoRoent	6921255CP2	FDA UDI	Class II	Active
ReLine	13065510	FDA UDI	Class II	Active
Armada	8461602	FDA UDI	Class II	Active
ReLine	13021045	FDA UDI	Class II	Active
VuePoint	7908240	FDA UDI	Class II	Active
CoRoent	5486565	FDA UDI	Class II	Active
ReLine	10100028	FDA UDI	Class II	Active
Xlif	2122215	FDA UDI	Class I	Active
CoRoent	5251344P2	FDA UDI	Class II	Active
CoRoent	5440400	FDA UDI	Class II	Active
CoRoent	5214305	FDA UDI	Class II	Active
ReLine	14460070	FDA UDI	Class II	Active
CoRoent	5122344	FDA UDI	Class II	Active
ReLine	16021010	FDA UDI	Class II	Active

Related Companies

Authorised Representatives

AJW Technology Consulting GmbH DE

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (36)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Date	Recall No.	Class	Status	Reason
Nov 10, 2022	Z-0738-2023	—	open, classified	Potential that insert will be unable to disengage from the vertebral body replacement device/implant
Jul 19, 2022	Z-1052-2023	—	open, classified	Due to an incorrect security key, customers were unable to connect to remote monitoring during spinal surgery, neck dissections, thoracic surgeries, and upper and lower extremity procedures.
Jun 20, 2022	Z-1453-2022	—	open, classified	Cervical artificial disc Unique Device Identifier (UDI) barcodes contain the incorrect Global Trade Item Number (GTIN) on the Patient Label when scanned and may also contain the incorrect GTIN human readable text, which could lead to selecting an incorrectly sized unit.
Jun 10, 2020	Z-2684-2020	—	terminated	The NVM5 EMG Module kit intended for intraoperative neurophysiologic monitoring during spinal surgery contains incorrect component, part number 1715945, SSEP harness instead of the the correct part number 1747065, NVM5 Harness, Gen 3.5 EM. This issue can result in delay in therapy or lack of EMG neuromonitoring during surgery if the surgeon elects to proceed without the NVM5.
Feb 13, 2020	Z-1898-2020	—	terminated	Post-implantation separation of an actuator end cap component that may expose internal components of the actuator, which could lead to hastened degeneration of the internal components and egress of Titanium alloy wear debris and resultant localized tissue discoloration.
Jan 5, 2009	Z-0369-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0361-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0351-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0370-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0375-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0348-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0354-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0377-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0355-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0374-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0378-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0352-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0372-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0363-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0350-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0364-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0367-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0359-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0366-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0373-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0362-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0349-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0360-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0353-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0365-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0376-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0371-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0357-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0358-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0368-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0356-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.